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Pramipexole dihydrochloride

NDC 68462-334 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA090781
Dosage form / routeTABLET · ORAL
Active ingredientsPRAMIPEXOLE DIHYDROCHLORIDE (1.5 mg/1)
Marketing started20101008
Package count3

External sources

Source: openFDA. Public-domain (CC0).